project manager

hr manager

qa automation engineer

quality control incharge

sqa engineer

quality control manager

JOFA Group

We are looking for a motivated QC Manager to lead our quality control processes and ensure our products meet the highest standards.Responsibilities<ul><li>Oversee quality control from raw materials to finished garments</li><li>Conduct inspections of fabrics, trims, samples, and bulk production</li><li>Monitor vendor and factory compliance with brand standards</li><li>Identify and resolve quality issues in collaboration with production and design teams</li><li>Manage QC staff and provide training where needed</li><li>Maintain reports and records on QC performance</li><li>Ensure compliance with sustainability and safety standards</li></ul>Requirements<ul><li>Bachelor&rsquo;s degree in Textile Engineering, Apparel Production, or related field (preferred)</li><li>5+ years&rsquo; experience in QC/QA within the fashion or apparel industry</li><li>Strong knowledge of fabrics, garment construction, and production methods</li><li>Experience managing vendors and conducting factory audits</li><li>Excellent problem-solving, organizational, and communication skills</li><li>Ability to work in a fast-paced environment with attention to detail</li></ul>Job Type: Full-timeWork Location: In person

QC Manager

Barqtron Engineering Solutions

We are seeking an experienced QA/QC Manager to take charge of our quality assurance and control initiatives. This role will ensure adherence to project specifications, company policies, and relevant industry standards throughout the engineering, procurement, and construction lifecycle.Key Responsibilities:<ul><li>Develop and sustain a Quality Management System (QMS) in alignment with recognized standards such as ISO 9001, ISO 13485, AS9100, and IATF 16949.</li><li>Perform internal quality audits and assist with audits conducted by customers, regulatory bodies, or third parties.</li><li>Prepare, revise, and maintain quality-related documentation, including procedures, policies, and templates.</li><li>Manage corrective and preventive actions (CAPAs), drive process enhancements, and conduct root cause analyses.</li><li>Facilitate training programs to promote understanding and implementation of quality practices and methodologies.</li><li>Track and analyze quality metrics; manage non-conformance reports and ensure effective resolution.</li><li>Collaborate on validation efforts and coordinate with suppliers to resolve quality concerns.</li></ul>Qualifications:<ul><li>Bachelor&rsquo;s degree in Engineering or a related discipline.</li><li>2&ndash;5 years of hands-on experience in quality systems or quality management roles.</li><li>Working knowledge of quality frameworks and tools such as Six Sigma, Lean principles, CAPA, and 8D.</li><li>Excellent communication, problem-solving, and organizational skills.</li><li>Proficiency in Microsoft Office and quality management software; internal auditing credentials are advantageous.</li><li>Background in document control, production environments, and regulatory compliance (FDA, EASA, OEMs).</li><li>Certifications like Certified Quality Engineer (CQE) or Certified Quality Auditor (CQA) are highly desirable.</li></ul>Job Type: Full-timeWork Location: In person

Manager QA/QC

Continental Print & Pack (Pvt) Ltd

Responsibilities:&middot; Check &amp; review all QC parameters as per requirement before production, during production &amp; after production and ensure all results are within specifications.&middot; Conduct Inspection of all incoming materials such as cores, cartons, inks, solvents and films.&middot; Make sure all dimensions and requirements of material should be according to the supplier&rsquo;s COA.&middot; Conduct ink testing which involves checking (viscosity, specific gravity &amp; solid content) to ensure ink quality and performance.&middot; Responsible for making shades for every new job as per customer provided sample or Epson.&middot; Carry out lab test for Raw material, semi-finished and finished material as per requirement.&middot; Documents results of testing and analyze data.&middot; Perform Bonding and Sealing Strength inspections for Semi-finished and Finished goods.&middot; Operate X-Rite Spectrophotometer to control Shade variations and perform new color/ink shades development as per requirement.&middot; Operate &amp; maintain laboratory equipment such as Tensile Machine, Heat sealer, Leak Tester, etc. to evaluate product durability, sealing efficacy and integrity.&middot; Observing and reporting any kind of process deviation to immediate supervisors and QAQC manager.&middot; Communicate with supplier regarding complaints and align visits if needed.&middot; Documents inspection results by completing reports and logs, summaries and inputs data into quality data base.&middot; Maintain sample retention system as per Company Policy.&middot; Follow Company Policies, procedures, HSE, food safety protocols and core processes as defined by the organization within daily working routine.&middot; Performs other duties and tasks as allocated by A.M QA/QC and above in the reporting line.Qualification &amp; Experience:&middot; Thorough knowledge of Food Safety, Halal Food Management Systems &amp; Quality Management Systems.&middot; 1-2 years of relevant work experience in the same field.&middot; Technical understanding of quality parameters and equipment &amp; machines.&middot; Strong organizational skills with excellent attention to details.&middot; Good writing, analytical and problem-solving skills.&middot; Ability to work independently and as part of a team.&middot; Strong mathematical skills with an ability to spot numerical errors.&middot; Good working knowledge of databases and systems.&middot; Proficiency in computers (Ms. Excel, Ms. PowerPoint, Ms. Word).&middot; Ability to work under pressure and meet deadlines.Job Type: Full-timeWork Location: In person

QAQC Executive

<div>Site Name: Pakistan - Sindh - Karachi 
Posted Date: Oct 6 2025 
Job Purpose
To supervise the quality control activities of Lab Operations &amp; ensure compliance as per cGMP, regulatory and QMS requirements for Site F-268.
Quality Control Incharge role is responsible for the requirements in accordance with the Local Regulations.
Education, Experience &amp; Skills<ul><li>
M.Sc. Chemistry or Pharm-D</li><li>
Minimum 10-years&rsquo; experience of testing for M.Sc. Chemistry / Pharmacist of having 6 years&rsquo; experience of testing.</li><li>
Computer literacy, minimum to access and utilize emails for official correspondence.</li><li>
Use of MS-Office (Word, Excel, PowerPoint) at least to a moderate level.</li><li>
Stakeholder management and good communication skills.</li><li>
Stay updated with the latest local regulatory standards and pharmacopoeia requirements and guidelines related to QC in the pharmaceutical industry.</li><li>
Ability to work in a fast-paced, highly regulated environment.</li><li>
Experience leading teams and managing laboratory operations</li></ul>
Key Responsibilities<ul><li>
Oversight for the testing and release / rejection of incoming materials, intermediate, bulk, and finished products, and batch records for site and for contract manufacturing.</li><li>
Oversee the Quality control processes, including sampling, testing and inspection of raw material, finished Products &amp; Utilities. Oversee specifications, test methods, and other quality control procedures. Ensure analysis is being carried out in compliance with the standards in case of any contract</li><li>
Perform &amp; review of current standard related to QMS and local regulatory for Quality Control Lab.</li><li>
Perform and approve appropriate validations pertaining to Lab ops, including those of analytical procedures, cleaning method validation &amp; Equipment validations. Ensure routine cleaning verification on time.</li><li>
Ensure timely completion of equipment calibrations and ensure DI Compliance</li><li>
Oversee the maintenance of the department, premises, and equipment.</li><li>
Oversight that the initial and continuing training of Quality personnel is carried out and adapted according to need Lead self-inspection process for the governance of Quality system in compliance with QMS and Local regulatory requirements.</li><li>
Responsible for the management and timely updation of legal agreements, quality agreements, and also responsible for third-party risk management.</li><li>
Ensure timely creation, submission, and approval of purchase orders to facilitate the availability of laboratory consumables and CAPEX items, ensuring uninterrupted laboratory operations.</li><li>
Provide support to ensure the timely preparation and submission of responses pertaining to laboratory operations for regulatory queries</li></ul>
Why GSK? 
Uniting science, technology and talent to get ahead of disease together.
GSK is a global biopharma company with a purpose to unite science, technology and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by the end of the decade, as a successful, growing company where people can thrive. We get ahead of disease by preventing and treating it with innovation in specialty medicines and vaccines. We focus on four therapeutic areas: respiratory, immunology and inflammation; oncology; HIV; and infectious diseases &ndash; to impact health at scale.
People and patients around the world count on the medicines and vaccines we make, so we&rsquo;re committed to creating an environment where our people can thrive and focus on what matters most. Our culture of being ambitious for patients, accountable for impact and doing the right thing is the foundation for how, together, we deliver for patients, shareholders and our people.
Contact information:
You may apply for this position online by selecting the Apply now button.
Important notice to Employment businesses/ Agencies
GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK's commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site.</div>

Quality Control Incharge

<div>
 
 Site Name:
 
 Pakistan - Sindh - Karachi
 
 
 
 Posted Date:
 
 Oct 6 2025
 
 
 
 Job Purpose
 
 
 
 To supervise the quality control activities of Lab Operations &amp; ensure compliance as per cGMP, regulatory and QMS requirements for Site F-268.
 
 
 Quality Control Incharge role is responsible for the requirements in accordance with the Local Regulations.
 
 
 
 Education, Experience &amp; Skills
 
 
 
 
 <ul>
 <li>
 M.Sc. Chemistry or Pharm-D
 </li>
 <li>
 Minimum 10-years&rsquo; experience of testing for M.Sc. Chemistry / Pharmacist of having 6 years&rsquo; experience of testing.
 </li>
 <li>
 Computer literacy, minimum to access and utilize emails for official correspondence.
 </li>
 <li>
 Use of MS-Office (Word, Excel, PowerPoint) at least to a moderate level.
 </li>
 <li>
 Stakeholder management and good communication skills.
 </li>
 <li>
 Stay updated with the latest local regulatory standards and pharmacopoeia requirements and guidelines related to QC in the pharmaceutical industry.
 </li>
 <li>
 Ability to work in a fast-paced, highly regulated environment.
 </li>
 <li>
 Experience leading teams and managing laboratory operations
 
 
 
 </li>
 </ul>
 
 Key Responsibilities
 
 
 
 
 <ul>
 <li>
 Oversight for the testing and release / rejection of incoming materials, intermediate, bulk, and finished products, and batch records for site and for contract manufacturing.
 </li>
 <li>
 Oversee the Quality control processes, including sampling, testing and inspection of raw material, finished Products &amp; Utilities. Oversee specifications, test methods, and other quality control procedures. Ensure analysis is being carried out in compliance with the standards in case of any contract
 </li>
 <li>
 Perform &amp; review of current standard related to QMS and local regulatory for Quality Control Lab.
 </li>
 <li>
 Perform and approve appropriate validations pertaining to Lab ops, including those of analytical procedures, cleaning method validation &amp; Equipment validations. Ensure routine cleaning verification on time.
 </li>
 <li>
 Ensure timely completion of equipment calibrations and ensure DI Compliance
 </li>
 <li>
 Oversee the maintenance of the department, premises, and equipment.
 </li>
 <li>
 Oversight that the initial and continuing training of Quality personnel is carried out and adapted according to need Lead self-inspection process for the governance of Quality system in compliance with QMS and Local regulatory requirements.
 </li>
 <li>
 Responsible for the management and timely updation of legal agreements, quality agreements, and also responsible for third-party risk management.
 </li>
 <li>
 Ensure timely creation, submission, and approval of purchase orders to facilitate the availability of laboratory consumables and CAPEX items, ensuring uninterrupted laboratory operations.
 </li>
 <li>
 Provide support to ensure the timely preparation and submission of responses pertaining to laboratory operations for regulatory queries
 
 
 
 </li>
 </ul>
 
 Why GSK?
 
 
 Uniting science, technology and talent to get ahead of disease together.
 
 
 
 GSK is a global biopharma company with a purpose to unite science, technology and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by the end of the decade, as a successful, growing company where people can thrive. We get ahead of disease by preventing and treating it with innovation in specialty medicines and vaccines. We focus on four therapeutic areas: respiratory, immunology and inflammation; oncology; HIV; and infectious diseases &ndash; to impact health at scale.
 
 
 People and patients around the world count on the medicines and vaccines we make, so we&rsquo;re committed to creating an environment where our people can thrive and focus on what matters most. Our culture of being ambitious for patients, accountable for impact and doing the right thing is the foundation for how, together, we deliver for patients, shareholders and our people.
 
 
 
 Contact information:
 
 
 
 You may apply for this position online by selecting the
 
 Apply now
 
 button.
 
 
 
 Important notice to Employment businesses/ Agencies
 
 
 
 GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK's commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site.
</div>

Three Horse Collections

Position Title: Production Manager Location: Karachi (Manufacturing Facility)Role Summary: We are looking for an experienced Production Manager to establish and oversee manufacturing operations for a new consumer goods product line in the nicotine category. The ideal candidate should have experience in FMCG or pharmaceutical production and the ability to set up efficient, compliant production systems from scratch.Key Responsibilities:<ul><li>Set up and manage production lines, ensuring GMP compliance.</li><li>Develop and monitor production plans, quality control, and output targets.</li><li>Manage material procurement, inventory, and supplier coordination.</li><li>Implement safety and hygiene standards in the production area.</li><li>Supervise production staff and ensure efficient workflow.</li><li>Collaborate with R&amp;D for formulation and product consistency.</li></ul>Key Performance Indicators (KPIs):<ul><li>Production output &ge; 95% of target.</li><li>Quality defect rate &le; 1%.</li><li>Zero safety violations.</li><li>On-time order fulfillment &ge; 98%.</li></ul>Requirements:<ul><li>Bachelor&rsquo;s in Industrial, Chemical, or Mechanical Engineering.</li><li>5&ndash;8 years of production management experience in FMCG/pharma manufacturing.</li><li>Strong process setup and operational leadership skills.</li><li>Familiarity with regulatory standards (ISO, GMP, health &amp; safety).</li><li>Hands-on approach with a focus on quality and efficiency.</li></ul>Job Type: Full-timePay: From Rs100,000.00 per monthApplication Question(s):<ul><li>What is your current/expected monthly salary?</li><li>Are you familiar with quality control and compliance procedures for consumer goods?</li><li>Have you worked in regulated industries such as nicotine, tobacco, or pharmaceuticals?</li></ul>Education:<ul><li>Bachelor's (Required)</li></ul>Experience:<ul><li>production management: 5 years (Required)</li></ul>Location:<ul><li>Karachi (Required)</li></ul>Work Location: In person

Production Manager - Consumer Product (Nicotine Pouches)

HRSG

<ul><li>Lead and manage all civil and MEP construction activities for the control center and associated infrastructure.</li><li>Oversee and coordinate all subsystems integration, including Automation systems, Telecom, Electrical, and Control Systems.</li><li>Supervise and guide the entire site team, including engineers, supervisors, and subcontractors.</li><li>Manage all interfaces and coordination with:</li><li>Site execution teams</li><li>Testing &amp; Commissioning (T&amp;C) teams</li><li>Procurement and logistics</li><li>Warehouse and material control</li><li>Quality assurance and control</li><li>Health, Safety &amp; Environment (HSE)</li><li>Site security teams</li><li>Ensure proper sequencing, interface alignment, and integration of all technical systems.</li><li>Maintain strong relationships with subcontractors and ensure performance, compliance, and accountability.</li><li>Ensure strict adherence to HSE standards and conduct regular safety audits.</li><li>Monitor and enforce quality control procedures and ensure compliance with project specifications.</li><li>Prepare and issue site progress reports, including daily, weekly, and monthly updates.</li><li>Oversee and support Testing &amp; Commissioning (T&amp;C) of all systems and infrastructure.</li><li>Manage the client handover process, including documentation, punch list clearance, and final acceptance.</li><li>Coordinate and verify site-related invoicing, ensuring alignment with progress and contractual milestones.</li><li>Manage the relationship with client and ensure alignment on technical and operational matters.</li><li>Resolve technical and operational issues on-site and escalate critical matters as needed.</li></ul>Job Types: Full-time, Contract Contract length: 12 monthsPay: From Rs300,000.00 per monthExperience:<ul><li>control room project manager: 10 years (Required)</li></ul>Work Location: In person

Control Room Site Manager

Explore 1227+ Quality control manager in Karachi this October. Find roles across top companies and apply now to boost your career.

1227 quality control manager jobs IN Karachi

QC Manager

Manager QA/QC

QAQC Executive

Quality Control Incharge

Quality Control Incharge

Production Manager - Consumer Product (Nicotine Pouches)

Control Room Site Manager